NSC59984 (803647-40-7) is a p53 activator. Restores wild-type p53 signaling and depletes mutant p53 gain of function. Induces mutant p53 protein degradation via MDM2 and ubiquitin-proteasome pathway. Induces p73-dependent cell death in cancer cells without toxicity toward normal cells.1Inhibition of p53-MDM2 interaction remains a viable strategy for cancer therapeutic development.2,3
NSC59984 induces mutant p53 protein degradation via MDM2 and the ubiquitin-proteasome pathway[1]. NSC59984 acts by targeting GOF-mutant p53 and stimulates p73 to restore the p53 pathway signaling[2].
in sw480 and dld-1 cells, nsc59984 treatment for 3 hours dose-dependently increased the mrna levels of p21, noxa and puma. nsc59984 was also found to increase p53-responsive reporter activity in both sw480 in a dose-dependent manner. the ec50 values of nsc59984 against a panel of cancer cell lines were different, varying from 8.38 to 110.49 μm. after incubation with 12 μm nsc59984 for 8 hours, the level ofγh2ax, a marker of genotoxicity due to dna double-strand breaks, increased in hct116 cells. nsc59984 induced cell death in apanel of cancer cells but displayed little or no cytotoxicity towards normal cells.noxa mrna slightly increased in response to 25 μm of nsc59984 in hct116 and 12 μm of nsc59984 in p53-null hct116 cells [1].
in nude mice bearing colon-tumor xenografts, nsc59984 (i.p. injection, 45mg/kg) did not cause an obvious change in mouse body weights and no overt toxic effects. nsc59984 treatment significantly repressed the dld-1 xenograft tumor growth. tumor weight measured at day 15 reduced by 34% in dld-1 xenograft tumors. in p73 knock-down dld-1 xenograft tumors, nsc59984 didn’t suppress tumor growth. in p73 knock-down dld-1 xenograft tumors, nsc59984 treatment reduced tumor weight by 18% [1].
[1] SHENGLIANG ZHANG. Small-Molecule NSC59984 Restores p53 Pathway Signaling and Antitumor Effects against Colorectal Cancer via p73 Activation and Degradation of Mutant p53.[J]. Cancer research, 2015, 75 18: 3842-3852. DOI:
10.1158/0008-5472.can-13-1079[2] MARIA FERRAIUOLO. Oncogenic Intra-p53 Family Member Interactions in Human Cancers.[J]. Frontiers in Oncology, 2016: 77. DOI:
10.3389/fonc.2016.00077[3] BO HONG. Targeting tumor suppressor p53 for cancer therapy: strategies, challenges and opportunities.[J]. Current drug targets, 2014, 15 1: 80-89. DOI:
10.2174/1389450114666140106101412
